ClinVar Miner

List of variants in gene LIFR reported as benign for not provided

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Gene type:
ClinVar version:
Total variants: 84
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HGVS dbSNP gnomAD frequency
NM_001127671.2(LIFR):c.*362G>A rs1005017 0.70336
NM_001127671.2(LIFR):c.2671-184G>A rs2256595 0.46511
NM_001127671.2(LIFR):c.397+29A>C rs2289779 0.37791
NM_001127671.2(LIFR):c.*1470T>G rs13156520 0.30679
NM_001127671.2(LIFR):c.*5670A>G rs3822425 0.30662
NM_001127671.2(LIFR):c.*6190C>T rs1046224 0.30641
NM_001127671.2(LIFR):c.*3834C>G rs34130318 0.30347
NM_001127671.2(LIFR):c.562-88A>G rs1037033 0.30225
NM_001127671.2(LIFR):c.561+216A>G rs1822815 0.30148
NM_001127671.2(LIFR):c.1292-80T>A rs16903989 0.29875
NM_001127671.2(LIFR):c.1672-82G>A rs3729741 0.29783
NM_001127671.2(LIFR):c.1885+222A>G rs2162885 0.29596
NM_001127671.2(LIFR):c.*5169T>A rs3822426 0.18293
NM_001127671.2(LIFR):c.2353G>A (p.Val785Ile) rs3110234 0.17829
NM_001127671.2(LIFR):c.2167+21T>C rs3110971 0.17819
NM_001127671.2(LIFR):c.*586A>T rs2561819 0.10855
NM_001127671.2(LIFR):c.398-56A>G rs3729598 0.06976
NM_001127671.2(LIFR):c.*4854A>G rs35853268 0.06740
NM_001127671.2(LIFR):c.2065+142C>T rs62353655 0.04077
NM_001127671.2(LIFR):c.143-60A>G rs62355821 0.04013
NM_001127671.2(LIFR):c.1672-148C>T rs2561826 0.04005
NM_001127671.2(LIFR):c.1672-180C>T rs2561827 0.03991
NM_001127671.2(LIFR):c.346C>T (p.His116Tyr) rs3729734 0.03927
NM_001127671.2(LIFR):c.*5225C>T rs58755763 0.03718
NM_001127671.2(LIFR):c.*4243A>G rs73749255 0.03708
NM_001127671.2(LIFR):c.2671-158_2671-157insTTTT rs1278539486 0.03440
NM_001127671.2(LIFR):c.2671-149_2671-148insTCCG rs1437530857 0.03436
NM_001127671.2(LIFR):c.2671-152del rs1220261200 0.03436
NM_001127671.2(LIFR):c.2671-150A>T rs1338198293 0.03435
NM_001127671.2(LIFR):c.2671-143_2671-119del rs1405234004 0.03427
NM_001127671.2(LIFR):c.991+80G>T rs6451387 0.03281
NM_001127671.2(LIFR):c.2498-243G>T rs75261849 0.03256
NM_001127671.2(LIFR):c.258-132G>A rs16903991 0.03242
NM_001127671.2(LIFR):c.1438-117G>A rs7701409 0.02036
NM_001127671.2(LIFR):c.992-246A>G rs73749259 0.01934
NM_001127671.2(LIFR):c.1291+252A>G rs58036502 0.01744
NM_001127671.2(LIFR):c.1671+261T>C rs11956342 0.01543
NM_001127671.2(LIFR):c.1886-18C>T rs3729743 0.01528
NM_001127671.2(LIFR):c.1937C>A (p.Thr646Asn) rs79040751 0.00875
NM_001127671.2(LIFR):c.*394C>A rs115958115 0.00870
NM_001127671.2(LIFR):c.1732G>A (p.Asp578Asn) rs3729740 0.00852
NM_001127671.2(LIFR):c.1899A>G (p.Ile633Met) rs2303743 0.00702
NM_001127671.2(LIFR):c.1991C>T (p.Ser664Leu) rs3729744 0.00642
NM_001127671.2(LIFR):c.2766T>C (p.Asp922=) rs61027880 0.00501
NM_001127671.2(LIFR):c.2591+17T>C rs73077453 0.00459
NM_001127671.2(LIFR):c.954C>T (p.Thr318=) rs61748202 0.00421
NM_001127671.2(LIFR):c.420G>A (p.Glu140=) rs142475175 0.00380
NM_001127671.2(LIFR):c.789A>G (p.Val263=) rs141925289 0.00321
NM_001127671.2(LIFR):c.2498-7G>A rs113078097 0.00306
NM_001127671.2(LIFR):c.2447A>G (p.Asp816Gly) rs74856317 0.00245
NM_001127671.2(LIFR):c.2578C>T (p.Arg860Trp) rs146205670 0.00066
NM_001127671.2(LIFR):c.1915A>T (p.Met639Leu) rs143808825 0.00064
NM_001127671.2(LIFR):c.774T>C (p.Asp258=) rs761633332 0.00016
NM_001127671.2(LIFR):c.1722G>A (p.Ser574=) rs200521119 0.00008
NM_001127671.2(LIFR):c.2497+14T>G rs541984532 0.00004
NM_001127671.2(LIFR):c.3060G>A (p.Glu1020=) rs537706381 0.00001
NM_001127671.2(LIFR):c.*3330C>A rs148827994
NM_001127671.2(LIFR):c.1292-19_1292-18del rs564274522
NM_001127671.2(LIFR):c.1417T>C (p.Ser473Pro) rs543824186
NM_001127671.2(LIFR):c.142+122del rs11293177
NM_001127671.2(LIFR):c.143-37GT[10] rs10637374
NM_001127671.2(LIFR):c.143-37GT[12] rs10637374
NM_001127671.2(LIFR):c.143-37GT[13] rs10637374
NM_001127671.2(LIFR):c.143-37GT[15] rs10637374
NM_001127671.2(LIFR):c.143-37GT[16] rs10637374
NM_001127671.2(LIFR):c.143-37GT[17] rs10637374
NM_001127671.2(LIFR):c.143-39_143-28del rs3836782
NM_001127671.2(LIFR):c.143-5_143-3del rs778581246
NM_001127671.2(LIFR):c.1600+17A>G
NM_001127671.2(LIFR):c.1601-3del rs776524743
NM_001127671.2(LIFR):c.1671+18C>T
NM_001127671.2(LIFR):c.1672-6dup
NM_001127671.2(LIFR):c.2336-4dup rs2112378006
NM_001127671.2(LIFR):c.2592-9del
NM_001127671.2(LIFR):c.2671-162T>G rs573391870
NM_001127671.2(LIFR):c.3288C>T (p.Asn1096=) rs3729751
NM_001127671.2(LIFR):c.397+17_397+20del rs139143276
NM_001127671.2(LIFR):c.561+212G>A rs7727565
NM_001127671.2(LIFR):c.562-3del
NM_001127671.2(LIFR):c.737-13dup rs2112493883
NM_001127671.2(LIFR):c.737-15T>C
NM_001127671.2(LIFR):c.991+84del rs34968906
NM_001127671.2(LIFR):c.992-8del
NM_001127671.2(LIFR):c.992-8dup rs773048780

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